| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:207617260-207617477 | Common:1; Rare:29 | ||||
| chr2:207743611-207743795 | Rare:41 | ||||
| chr2:207747401-207747689 | Common:2; Rare:54 | ||||
| chr2:207973218-207973462 | Common:1; Rare:38 | ||||
| chr2:207984777-207984974 | Common:1; Rare:24 | ||||
| chr2:208273425-208273623 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr2:208306939-208307153 | Common:2; Rare:42 | ||||
| chr2:208851021-208851034 | |||||
| chr2:209424845-209424934 | Rare:14 | ||||
| chr2:209508557-209508824 | Common:4; Rare:62 | ||||
| chr2:210006010-210006062 | Rare:7 | ||||
| chr2:210024156-210024449 | Common:2; Rare:71 | ||||
| chr2:210027339-210027455 | Rare:30 | ||||
| chr2:210028712-210028751 | Rare:8 | ||||
| chr2:210049276-210049321 | Rare:17 |